US9738727B2 - Anti-HtrA1 antibodies and methods of use - Google Patents
Anti-HtrA1 antibodies and methods of use Download PDFInfo
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- US9738727B2 US9738727B2 US13/651,289 US201213651289A US9738727B2 US 9738727 B2 US9738727 B2 US 9738727B2 US 201213651289 A US201213651289 A US 201213651289A US 9738727 B2 US9738727 B2 US 9738727B2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/40—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against enzymes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/34—Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
- C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
Definitions
- Dysregulated TGF- ⁇ signaling by aberrant HtrA1 expression may also contribute to arthritic disease (Oka, C., et al., Development 131:1041-53 (2004); Tsuchiya, A., et al., Bone 37:323-36 (2005)), perhaps in conjunction with HtrA1-mediated degradation of various extracellular matrix components (Chamberland et al., J Biol Chem 284:27352-9 (2009); Grau, S., et al., J Biol Chem 281:6124-9 (2006); Hadfield, K.
- an antibody described herein comprises (a) HVR-H1 comprising the amino acid sequence GFX l IX m X n YY, wherein X l is N, S or T; X m is S, D, Y or A; and X n is G or D (SEQ ID NO:87); (b) HVR-H2 comprising the amino acid sequence WIDPYGGDTX o , wherein X o is N or D (SEQ ID NO:88); (c) HVR-H3 comprising the amino acid sequence GTFLTX p WGHY, wherein X p is S or T (SEQ ID NO: 89); (d) HVR-L1 comprising the amino acid sequence X a X b X c X d X e X f , wherein X a is D, S or V; X b is V or I; X c is S, N or G; X d is T or N; X
- FIG. 5 Specificity of IgG94.
- MuHtrA1_PD, MuHtrA3_PD and MuHtrA4_PD were incubated with increasing concentrations of IgG94 and enzyme activities towards the peptide substrate H2-Opt (top panel) or casein BODIPY FL reagent (bottom panel) determined and expressed as percentage of uninhibited enzyme activities (% of control)
- antibody herein is used in the broadest sense and encompasses various antibody structures, including but not limited to monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies), and antibody fragments so long as they exhibit the desired antigen-binding activity.
- an anti-HtrA1 antibody has one or more of the following properties: (i) has an IC 50 of less than 50 nM, 30 nM, 25 nM, 20 nM, 15 nM, 10 nM, 5 nM, 3 nM, 2.5 nM, 2 nM, 1 nM, or less for one or more HtrA1 substrates; (ii) binds to HtrA1 with a ratio of 1 variable domain to one subunit of an HtrA1 trimer (e.g., a Fab binds to an HtrA1 trimer with a ratio of 3 Fab to 1 HtrA1 trimer, and an IgG binds to an HtrA1 trimer with a ratio of 3 IgG to 2 HtrA1 trimers), (iii) for antibodies comprising two variable domains, binds to HtrA1 in
- the invention provides an antibody comprising at least one, at least two, or all three VH HVR sequences selected from (a) HVR-H1 comprising an amino acid sequence selected from: SEQ ID NO:4, 20, 47-51 and 75-80; (b) HVR-H2 comprising an amino acid sequence selected from SEQ ID NO:5, 52 and 81-82; and (c) HVR-H3 comprising an amino acid sequence selected from: SEQ ID NO:6, 53 and 83-84.
- the antibody comprises HVR-H3 comprising an amino acid sequence selected from SEQ ID NO:6 and 53.
- the invention provides an antibody comprising at least one, at least two, or all three VH HVR sequences selected from (a) HVR-H1 comprising the amino acid sequence of SEQ ID NO:4; (b) HVR-H2 comprising the amino acid sequence of SEQ ID NO:5; and (c) HVR-H3 comprising the amino acid sequence of SEQ ID NO:6.
- the antibody comprises HVR-H3 comprising the amino acid sequence of SEQ ID NO:6.
- the antibody comprises HVR-H3 comprising the amino acid sequence of SEQ ID NO:6 and HVR-L3 comprising the amino acid sequence of SEQ ID NO:3.
- the invention provides an antibody comprising at least one, at least two, or all three VL HVR sequences selected from (a) HVR-L1 comprising the amino acid sequence of SEQ ID NO:21; (b) HVR-L2 comprising the amino acid sequence of SEQ ID NO:2; and (c) HVR-L3 comprising the amino acid sequence of SEQ ID NO:22.
- the antibody comprises (a) HVR-L1 comprising the amino acid sequence of SEQ ID NO:21; (b) HVR-L2 comprising the amino acid sequence of SEQ ID NO:2; and (c) HVR-L3 comprising the amino acid sequence of SEQ ID NO:22.
- the VH comprises one, two or three HVRs selected from: (a) HVR-H1 comprising an amino acid sequence selected from: SEQ ID NO:4, 20, 25 and 47-51, (b) HVR-H2 comprising an amino acid sequence selected from SEQ ID NO:5, 26 and 52, and (c) HVR-H3 comprising an amino acid sequence selected from SEQ ID NO:6, 27 and 53.
- Kd is measured using surface plasmon resonance assays using a BIACORE®-2000 or a BIACORE®-3000 (BIAcore, Inc., Piscataway, N.J.) at 25° C. with immobilized antigen CM5 chips at ⁇ 10 response units (RU).
- CM5 carboxymethylated dextran biosensor chips
- EDC N-ethyl-N′-(3-dimethylaminopropyl)-carbodiimide hydrochloride
- NHS N-hydroxysuccinimide
- an antibody provided herein is an antibody fragment.
- Antibody fragments include, but are not limited to, Fab, Fab′, Fab′-SH, F(ab′) 2 , Fv, and scFv fragments, and other fragments described below.
- Fab fragment antigen
- Fab′ fragment antigen binding domain
- Fab′-SH fragment antigen binding domain antigen binding domain antigen binding domain antigen binding domain antigen binding domain antigen binding domains
- Fv fragment antigen binding domain antigen binding
- scFv fragments see, e.g., Pluckthün, in The Pharmacology of Monoclonal Antibodies , vol. 113, Rosenburg and Moore eds., (Springer-Verlag, New York), pp. 269-315 (1994); see also WO 93/16185; and U.S. Pat.
- Single-domain antibodies are antibody fragments comprising all or a portion of the heavy chain variable domain or all or a portion of the light chain variable domain of an antibody.
- a single-domain antibody is a human single-domain antibody (Domantis, Inc., Waltham, Mass.; see, e.g., U.S. Pat. No. 6,248,516 B1).
- some FR residues in a humanized antibody are substituted with corresponding residues from a non-human antibody (e.g., the antibody from which the HVR residues are derived), e.g., to restore or improve antibody specificity or affinity.
- a non-human antibody e.g., the antibody from which the HVR residues are derived
- an antibody provided herein is a human antibody.
- Human antibodies can be produced using various techniques known in the art. Human antibodies are described generally in van Dijk and van de Winkel, Curr. Opin. Pharmacol. 5: 368-74 (2001) and Lonberg, Curr. Opin. Immunol. 20:450-459 (2008).
- Human antibodies may be prepared by administering an immunogen to a transgenic animal that has been modified to produce intact human antibodies or intact antibodies with human variable regions in response to antigenic challenge.
- Such animals typically contain all or a portion of the human immunoglobulin loci, which replace the endogenous immunoglobulin loci, or which are present extrachromosomally or integrated randomly into the animal's chromosomes.
- the endogenous immunoglobulin loci have generally been inactivated.
- the carbohydrate attached thereto may be altered.
- Native antibodies produced by mammalian cells typically comprise a branched, biantennary oligosaccharide that is generally attached by an N-linkage to Asn297 of the CH2 domain of the Fc region. See, e.g., Wright et al. TIBTECH 15:26-32 (1997).
- alterations are made in the Fc region that result in altered (i.e., either improved or diminished) C1q binding and/or Complement Dependent Cytotoxicity (CDC), e.g., as described in U.S. Pat. No. 6,194,551, WO 99/51642, and Idusogie et al. J. Immunol. 164: 4178-4184 (2000).
- CDC Complement Dependent Cytotoxicity
- the immunuoconjugates or ADCs herein expressly contemplate, but are not limited to such conjugates prepared with cross-linker reagents including, but not limited to, BMPS, EMCS, GMBS, HBVS, LC-SMCC, MBS, MPBH, SBAP, SIA, SLAB, SMCC, SMPB, SMPH, sulfo-EMCS, sulfo-GMBS, sulfo-KMUS, sulfo-MBS, sulfo-SIAB, sulfo-SMCC, and sulfo-SMPB, and SVSB (succinimidyl-(4-vinylsulfone)benzoate) which are commercially available (e.g., from Pierce Biotechnology, Inc., Rockford, Ill., U.S.A).
- cross-linker reagents including, but not limited to, BMPS, EMCS, GMBS, HBVS, LC
- Antibodies of the invention can be used either alone or in combination with other agents in a therapy.
- an antibody of the invention may be co-administered with at least one additional therapeutic agent.
- an additional therapeutic agent is a therapeutic agent suitable for treatment of an ocular disorder associated with undesirable neovascularization in the eye, such as, for example, wet AMD.
- Suitable therapeutic agents include, for example, anti-angiogenic therapies such as an anti-VEGF therapy like LUCENTISTM (ranibizumab).
- an antibody of the invention when used alone or in combination with one or more other additional therapeutic agents, will depend on the type of disease to be treated, the type of antibody, the severity and course of the disease, whether the antibody is administered for preventive or therapeutic purposes, previous therapy, the patient's clinical history and response to the antibody, and the discretion of the attending physician.
- the antibody is suitably administered to the patient at one time or over a series of treatments.
- about 1 ⁇ g/kg to 15 mg/kg (e.g. 0.1 mg/kg-10 mg/kg) of antibody can be an initial candidate dosage for administration to the patient, whether, for example, by one or more separate administrations, or by continuous infusion.
- Synthetic antibody libraries displayed bivalent Fab fragments on the M13 phage and the diversity was generated by use of oligo-directed mutagenesis in three complementarity determining regions (CDRs) of the heavy chain.
- CDRs complementarity determining regions
- variable regions of both the heavy and light chains of Fab94 were subcloned into a E. coli Fab expression vector (AEP1).
- AEP1 E. coli Fab expression vector
- the resulting plasmid was transformed into E. coli . strain 34B8.
- the single colony was grown overnight at 37° C. in 30 ml LB medium supplemented with 50 ⁇ g/ml of Carbenicilin.
- Five ml of the culture was inoculated into 500 ml of complete C.R.A.P. medium (Simmons, L. C., et al., J Immunol Methods. 263:133-47 (2002)) supplemented with Carbenicilin (50 ⁇ g/ml) and grown at 30° C. for 24 h.
- the Fab94 protein was purified using protein A agarose resin.
- variable domains of both the light chain and heavy chain of Fab94 were cloned into a pRK5-based plasmid with human light chain or heavy chain (human IgG1) constant domain for transient expression in Chinese hamster ovary (CHO) cells.
- the IgG94 protein was purified by use of protein A agarose chromatography.
- HtrA1 was incubated in 96-well black optical bottom plates (Nalge Nunc Int., Rochester, N.Y.) with IgG94 or Fab94 serially diluted in 50 mM Tris-HCl, pH 8.0, 200 mM NaCl, 0.25% CHAPS (assay buffer) for 20 min at 37° C.
- IgG94 or Fab94 serially diluted in 50 mM Tris-HCl, pH 8.0, 200 mM NaCl, 0.25% CHAPS (assay buffer) for 20 min at 37° C.
- single concentrations of IgGs final concentrations 0.16 mg/ml-0.28 mg/ml were incubated with HuHtrA1 or HuHtrA1_PD.
- a 10 mM stock solution of the peptide substrate Mca-IRRVSYSF(Dnp)KK (SEQ ID NO:12) (H2-Opt) in DMSO was diluted in water to 12.5 ⁇ M, pre-warmed at 37° C. and then added to the reaction mixture.
- the final concentrations of the reactants were: 5 nM HuHtrA1 or MuHtrA1, 0.005-300 nM IgG94, 0.02-900 nM Fab94, 2.5 ⁇ M H2-Opt.
- control wells containing phage without biotinylated HuHtrA1 selection were captured on neutravidin-coated plates. Bound phage was eluted with 0.1N HCl for 20 min, neutralized by 1/10 volume of 1M Tris pH11, titered, and propagated for the next round.
- three more rounds of solution sorting were carried out using two methods of increasing selection stringency simultaneously. The first method, which is for on-rate selection, decreases biotinylated target protein concentration from 10 nM to 0.1 nM. The second method, which is for off-rate selection, adds excess amounts of non-biotinylated HuHtrA1 protein (100 ⁇ 1000 fold more) to compete off weaker binders. Also, the phage input was decreased (0.1 ⁇ 0.5 O.D/ml) to lower the background phage binding.
- Recombinant murine HtrA1 standard (Genentech) and samples from rat or murine tissues were diluted in sample/standard dilution buffer (PBS, 0.5% BSA, 15 ppm Proclin, 0.05% Tween 20, 0.25% CHAPS, 0.2% BgG, 5 mM EDTA, 0.35M NaCl, (pH 7.4)), added to washed plates, and incubated for 1.5-2 hours.
- sample/standard dilution buffer PBS, 0.5% BSA, 15 ppm Proclin, 0.05% Tween 20, 0.25% CHAPS, 0.2% BgG, 5 mM EDTA, 0.35M NaCl, (pH 7.4)
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US13/651,289 US9738727B2 (en) | 2011-10-14 | 2012-10-12 | Anti-HtrA1 antibodies and methods of use |
US15/653,201 US20170342163A1 (en) | 2011-10-14 | 2017-07-18 | ANTI-HtrA1 ANTIBODIES AND METHODS OF USE |
US16/143,098 US20190016826A1 (en) | 2011-10-14 | 2018-09-26 | ANTI-HtrA1 ANTIBODIES AND METHODS OF USE |
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US201161547649P | 2011-10-14 | 2011-10-14 | |
US13/651,289 US9738727B2 (en) | 2011-10-14 | 2012-10-12 | Anti-HtrA1 antibodies and methods of use |
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US15/653,201 Continuation US20170342163A1 (en) | 2011-10-14 | 2017-07-18 | ANTI-HtrA1 ANTIBODIES AND METHODS OF USE |
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US15/653,201 Abandoned US20170342163A1 (en) | 2011-10-14 | 2017-07-18 | ANTI-HtrA1 ANTIBODIES AND METHODS OF USE |
US16/143,098 Abandoned US20190016826A1 (en) | 2011-10-14 | 2018-09-26 | ANTI-HtrA1 ANTIBODIES AND METHODS OF USE |
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US16/143,098 Abandoned US20190016826A1 (en) | 2011-10-14 | 2018-09-26 | ANTI-HtrA1 ANTIBODIES AND METHODS OF USE |
Country Status (32)
Country | Link |
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US (3) | US9738727B2 (fr) |
EP (2) | EP3461839A1 (fr) |
JP (2) | JP6532678B2 (fr) |
KR (2) | KR20140082796A (fr) |
CN (2) | CN108373506A (fr) |
AR (1) | AR088322A1 (fr) |
AU (2) | AU2012322618A1 (fr) |
BR (1) | BR112014008862A2 (fr) |
CA (1) | CA2850032C (fr) |
CL (1) | CL2014000888A1 (fr) |
CO (1) | CO7020870A2 (fr) |
CR (1) | CR20140212A (fr) |
DK (1) | DK2766393T3 (fr) |
EA (1) | EA201490778A1 (fr) |
ES (1) | ES2687951T3 (fr) |
HK (1) | HK1255608A1 (fr) |
HR (1) | HRP20181457T1 (fr) |
HU (1) | HUE039133T2 (fr) |
IL (1) | IL232055B (fr) |
LT (1) | LT2766393T (fr) |
MA (1) | MA35712B1 (fr) |
MX (1) | MX2014004022A (fr) |
PE (1) | PE20141562A1 (fr) |
PL (1) | PL2766393T3 (fr) |
PT (1) | PT2766393T (fr) |
RS (1) | RS57645B1 (fr) |
SG (1) | SG11201401477XA (fr) |
SI (1) | SI2766393T1 (fr) |
TR (1) | TR201811270T4 (fr) |
TW (1) | TW201321414A (fr) |
WO (1) | WO2013055998A1 (fr) |
ZA (1) | ZA201402172B (fr) |
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JP2018534930A (ja) | 2015-10-30 | 2018-11-29 | ジェネンテック, インコーポレイテッド | 抗d因子抗体及びコンジュゲート |
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